Frontotemporal lobar degeneration – tau as a pied piper? Markus TolnayAlphonse Probst Review Article Pages: 63 - 75
Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice Sarah E. LloydJames B. UphillJohn Collinge Original Article Pages: 77 - 81
Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432 Marcy C. SpeerFelicia Lennon GrahamJeffery M. Vance Original Article Pages: 83 - 85
Congenital myasthenia in Brahman calves caused by homozygosity for a CHRNE truncating mutation Simone KranerJörn P. SiebOrtrud K. Steinlein Original Article Pages: 87 - 91
A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family Domna-Maria GeorgiouJanez ZidarKyproula Christodoulou Original Article Pages: 93 - 96
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease A. Bertoli Avella B. Marcheco Teruel P. Heutink Original Article Pages: 97 - 104
Multiple founder effects in Japanese families with primary torsion dystonia harboring the GAG deletion in the TOR1A (DYT1) gene Takeshi IkeuchiYoshiko NomuraShoji Tsuji Letter to the Editor Pages: 105 - 106
De novo MECP2 mutation in a 46,XX male patient with Rett syndrome Robert MaiwaldAnselm BöntePeter Herkenrath Letter to the Editor Pages: 107 - 108
